Skip to content

The Effect Of Self-Treatment Maneuver At Home In The Recovery Of Patients With Benign Paroxysmal Positional Vertigo

Investigating The effect Of Self-treatment Maneuver At Home In the Recovery of Patients With Benign Paroxysmal Positional Vertigo-A Clinical Trial Study

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
IRCT
Registry ID
IRCT20220608055103N2
Enrollment
86
Registered
2023-09-04
Start date
2023-09-23
Completion date
Unknown
Last updated
2023-10-16

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Benign Paroxysmal Positional Vertigo. Benign Paroxysmal Vertigo

Interventions

Intervention 1: Intervention group: the rehabilitation treatment of BPPV patients in the intervention group is done by using self-treatment positioning maneuver maneuvers at home . In this research,

Sponsors

Guilan University of Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 90 Years

Inclusion criteria

Inclusion criteria: A Diagnosis Of BPPV With Dix-Hallpike Maneuver And Clinical Signs No Previous Use Of Central Nervous System Depressants Or Stimulants In The Last 24 Hours

Exclusion criteria

Exclusion criteria: Other Causes Of Vertigo, Such As CPA Tumors, Anxiety Disorders, Confirmed Or Suspected Migraine A Disease Or Condition For Which The Self-Treatment Maneuver, Or The Epley Maneuver Was Contraindicated, Such As Degenerative Disorders Of The Cervical Or Thoracic Spine, Detachment Of The Retina, Myocardial Infarction, Or Severe Obesity Nystagmus That Indicates The Central Positional Nystagmus, Or Vestibular Migraine

Design outcomes

Primary

MeasureTime frame
Indicators Of Benign Paroxysmal Positional Vertigo According to DHI Scale. Timepoint: The Evaluation Of Patients Will Be Done Before Treatment And 1 Month Post-Treatment. Method of measurement: Dizziness Handicap Inventory Scale.

Secondary

MeasureTime frame
The level of patient satisfaction with the effect and comfort of the treatment performed based on the scale (Visual Analogue Scale). Timepoint: Before Treatment And One Month Post-Treatment. Method of measurement: Videonystagmography (VNG).

Countries

Iran (Islamic Republic of)

Contacts

Public ContactShadman Nemati

Guilan University of Medical Sciences

drshadmannemati_ent@yahoo.com+98 13 3323 8307

Outcome results

None listed

Source: IRCT (via WHO ICTRP) · Data processed: Feb 4, 2026